ENST00000578493.2:n.771C>G
|
|
|
ENST00000699291.1:c.563C>G
|
ENSP00000514272.1:p.Pro188Arg
|
|
ENST00000699292.1:n.478C>G
|
|
|
ENST00000225275.4:c.1438C>G
MANE Select
|
ENSP00000225275.3:p.Arg480Gly
|
|
ENST00000225275.3:c.1438C>G
|
ENSP00000225275.3:p.Arg480Gly
|
|
NM_000250.1:c.1438C>G , LRG_84t1:c.1438C>G
|
NP_000241.1:p.Arg480Gly
|
|
XM_011524821.1:c.1624C>G
|
XP_011523123.1:p.Arg542Gly
|
|
XM_011524822.1:c.1153C>G
|
XP_011523124.1:p.Arg385Gly
|
|
XM_011524823.1:c.1463C>G
|
XP_011523125.1:p.Pro488Arg
|
|
NM_000250.2:c.1438C>G
MANE Select
|
NP_000241.1:p.Arg480Gly
|
|